Development of tobacco varieties with no or significantly reduced anatabine content

Abstract

A process for producing a reduced tobacco-specific nitrosamine (TSNA) tobacco plant comprising reducing and/or eliminating anatabine biosynthesis in wild-type tobacco plant. In addition, use of such plants for discovery of molecular markers that are closely linked with genes required for anatabine biosynthesis and for discovery of genes required for anatabine biosynthesis. In addition, a smoking composition, a smoking article and a smokeless tobacco oral delivery product contain the tobacco material.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent Application Ser. No. 61/799,831, filed on Mar. 15, 2013, which is incorporated herein by reference in its entirety for all purposes.

BACKGROUND

Nicotiana tabacum produces several different pyridine alkaloids, with nicotine representing the most abundant. The alkaloids that accumulate to a lesser degree include anatabine, nornicotine, myosmine, and anabasine. These alkaloids are commonly referred to as minor alkaloids. Minor alkaloids are direct precursors in the formation of tobacco specific nitrosamines.

Nitrosamines and in particular, tobacco specific nitrosamines (TSNAs) are constituents of tobacco. Anatabine, a minor alkaloid, is nitrosated to form N′-nitrosoanatabine (NAT). NAT constitutes approximately 40% of total TSNAs. The biosynthesis of anatabine, and its associated genes, is not completely known. However, current understanding is that the synthesis of anatabine requires quinolinate phosphoribosyltransferease (QPT), a key enzyme regulating entry to the pyridine nucleotide cycle.

Biosynthesis of anatabine is thought to proceed via the conversion of nicotinic acid to 3,6-dihydronicotinic acid. After decarboxylation to produce 3,6-dihydropyridine, and condensation with nicotinic acid to produce an intermediate, conversion to anatabine can occur by dehydrogenation. The current understanding of the alkaloid biosynthetic pathway is depicted in FIG. 1.

In addition to TSNAs, certain polyphenol compounds can form undesirable phenolic compounds during the combustion of tobacco and may also be targeted constituents of tobacco smoke. There is interest in providing a method for reducing the contents of these targeted compounds in tobacco.

BRIEF SUMMARY

The present disclosure significantly reduces and/or eliminates anatabine biosynthesis in tobacco. This prevents anatabine, a precursor of N′-nitrosoanatabine (NAT), from accumulating. NAT represents approximately 40% of total Tobacco Specific Nitrosamines (TSNAs), and as a result of elimination of anatabine as precursor, a 40% reduction in total TSNAs will be possible. This “ultra-low anatabine” trait can be combined with an ultra-low nornicotine trait in a tobacco line or variety to accomplish a further reduction of TSNA accumulation, as nornicotine is a precursor for N′-nitrosonornicotine formation. The combined ultra-low anatabine and ultra-low nornicotine traits could result in a reduction of total TSNAs on the order of about 70-80%.

The present disclosure details the development of an ultra-low anatabine trait through induced variation (EMS treatment) followed by a screen for plants deficient in anatabine. The ultra-low anatabine trait can be crossed into other commercial varieties, or the trait can be induced in a similar fashion directly into commercial tobacco varieties.

Currently there is no commercially relevant tobacco variety with reduced anatabine in leaf lamina. Since anatabine is a precursor for NAT which constitutes ˜40% of total TSNAs, this trait has applicability in producing tobacco with very low TSNAs for tobacco products.

The ultra-low anatabine plants are also ideal genetic material for discovery of molecular markers that are closely linked with genes required for anatabine biosynthesis, as well as the actual discovery of genes required for anatabine biosynthesis. As disclosed, a method for discovery of molecular markers that are closely linked with genes required for anatabine biosynthesis may comprise crossing a reduced TSNA tobacco plant with another tobacco plant, isolating genomic DNA from individual progeny of the cross, and detecting in the genomic DNA the presence or absence of a molecular marker that is closely linked with a gene required for anatabine biosynthesis. Also as disclosed, a method for discovery of genes required for anatabine biosynthesis may comprise crossing a reduced TSNA tobacco plant with another tobacco plant, isolating genomic DNA from individual progeny of the cross, and detecting in the genomic DNA the presence or absence of a gene required for anatabine biosynthesis

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts the alkaloid biosynthetic pathway.

FIG. 2 shows the reduction of anatabine content compared to other mutant lines.

FIG. 3 illustrates the percent anatabine content present in selected FC401 mutant lines at different generations.

FIG. 4 illustrates that the total anatabine content present in a selected TN90 LC mutant line at M2 and M3 generations.

FIG. 5 illustrates that the low anatabine FC401 M2 mutant line shows reduced NAT.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

As used herein, “tobacco material” denotes a tobacco starting material to be treated in various processes described herein, regardless of type, source or origin, which may have previously been subjected to other treatments. The tobacco material may include, but is not limited to, tobacco solids and any solid form of tobacco, such as, e.g., cured tobacco (such as flue-cured tobacco); uncured tobacco (also known as green tobacco); dried, aged, cut, ground, stripped or shredded tobacco; tobacco scrap; expanded tobacco; fermented tobacco; reconstituted tobacco; blended tobacco, etc. The tobacco material may be from any parts of the tobacco plant, such as leaf, stem, veins, scrap and waste tobacco, cuttings, etc.

In one embodiment, the smoking article is a cigarette.

Preferably, smokeless tobacco oral delivery products, such as chewing tobacco or pouched tobacco, are sized to comfortably be received in a human mouth. In addition, the oral products may be sized so that it can be moved around inside a human mouth.

A pouched tobacco typically contains an external wrapper and a tobacco material therein. The external wrapper preferably comprises a membrane that is sufficiently porous to allow passage through the membrane of a liquid, such as saliva, in the mouth. The external wrapper membrane is preferably resistant to deterioration in the presence of saliva and bacteria, and may be constructed from cellulose fiber such as tea bag material.

One embodiment provides a method of producing a reduced tobacco-specific nitrosamine (TSNA) tobacco plant comprising reducing and/or eliminating anatabine biosynthesis in wild-type tobacco plant. This may include preventing the accumulation of anatabine, the precursor of N′-nitrosoanatabine (NAT). This method may also comprise crossing said tobacco plant with reduced and/or eliminated anatabine biosynthesis with a tobacco plant having low nornicotine synthesis. A further embodiment is a reduced TSNA tobacco plant developed from these methods or a plant cell line produced from these methods. The TSNA levels can be reduced by at least about 40% when compared to a wild-type tobacco plant. Further envisioned is where the TSNA levels are reduced by at least about 70% when compared to a wild-type tobacco plant.

Another embodiment is the reduced TSNA tobacco plant in which a portion of said plant is used in a consumable tobacco product. This tobacco product can be, e.g., a cigarette or a smokeless tobacco product made from a reduced TSNA tobacco plant. Another embodiment is seeds from the reduced TSNA tobacco plant comprising reduced levels of anatabine.

Another embodiment provides a method for discovery of molecular markers that are closely linked with genes required for anatabine biosynthesis or discovery of genes required for anatabine biosynthesis comprising crossing a reduced tobacco-specific nitrosamine tobacco plant with another plant, isolating genomic DNA from individual progeny of the cross, and detecting in the genomic DNA the presence or absence of a molecular marker that is closely linked with a gene required for anatabine biosynthesis or a gene required for anatabine biosynthesis.

The embodiments disclosed herein are further illustrated by the following specific examples but is not limited hereto.

EXAMPLES

Example I

A novel genetic variation in a population of tobacco plants was created to identify plants that have lost the ability to biosynthesize anatabine. These plants are very likely to have a mutated non-functional version of one or more genes critical for anatabine biosynthesis. To induce novel genetic variation plants were treated with Ethyl methane sulfonate (EMS) and propagated to the M2 stage so that recessive mutations would express in plants homozygous for mutated genes.

A population of the Flue-cured variety “401” and TN90 was available for this investigation. Approximately 5000 seeds per variety were treated with 0.8% ethyl methane sulfonate and germinated. M1 plants were grown in the field and M2 seeds were collected. Approximately 2000 FC401 M2 and 500 TN90 M2 seeds were germinated and grown in 6″ pots. At 50% flowering stage, plants were topped and leaf samples were collected after 2 weeks of topping.

Alkaloids were extracted from the leaf samples: 1 ml methanol per gram tissue was added and sonicated for 30 minutes. The extract was centrifuged briefly to pellet the residual leaf tissue and purified extract was concentrated 10 times by vacuum centrifugation for approximately 75 minutes at 45° C. Five microliters of concentrated sample along with standards were loaded on HPTLC plates. After samples were dried for 20 minutes, the plate was transferred quickly into the developing chamber saturated with a solvent mixture of Toluene: Ethyl acetate: Diethylamine (5:4:1 respectively). The plate was run for approximately 10-15 minutes until the mobile phase ran through approximately 75% of the length of the plate. The plate was air dried and photographed under UV254 using a documentation system with video (CAMAG REPROSTAR 3). This image is reproduced in FIG. 2.

Alkaloid Analysis: Tobacco leaves were harvested and air-dried in an oven at 50° C. A one gram sample of crushed, dried leaf was added to 10 mL of 2 N NaOH in an extraction bottle. The sample was mixed and allowed to incubate for 15 minutes at room temperature. Alkaloids were extracted by the addition of 50 mL of extraction solution [0.04% quinolone (wt/vol) dissolved in methyl-tert-butyl ether] and gently rotated on a linear shaker for 3 hours. Following phase separation, an aliquot of the organic phase was transferred to a sample vial. Samples were analyzed using an Agilent 6890 Gas Chromatograph and 5973N Mass Spectrometer.

A total of 726 FC401 and 500 FN90 leaf samples were processed and screened for anatabine mutants. Mutant plants 97 (08GH97) and 153 (08GH153) in FIG. 2 show the reduction of anatabine content compared to other mutant lines. Using HPTLC screening and GCMS, 4 mutant lines were identified from FC401 and TN90 (Table 1). Mutants from MS108 (also referred to as dMS932), MF445 from FC401, and MS 3908 from TN90 mutant seeds were used for further analysis. Deposits of seeds of the dMS932 line have been made with the American Type Culture Collection (ATCC) and the accession number is ATCC Accession Number PTA-124990.

TSNA Analysis: Tobacco leaves were harvested and freeze-dried and powdered to 1 mm size. A 750 mg powdered sample was added to 30 mL of 100 mM ammonium acetate in a 60 mL amber vial. The sample was mixed and incubated in a shaker for 30 minutes. Approximately 4 mL of sample was transferred directly into labeled disposable culture tubes and 0.250 mL of concentrated ammonium hydroxide was added. The sample was vortexed for 1-5 seconds, after which time 1.5 mL of sample was added to a preconditioned extraction cartridge with a flow rate of 1-2 drops per second. Cartridges were washed and dried. Analytes from the extraction cartridges were eluted using 1.5 mL of 70:30 methanol:0.1% acetic acid and analyzed using liquid chromatography with tandem mass spectrometry (LC/MS/MS).

TABLE 1
Alkaloid Analysis by HPTLC and GC/MS
							Total
			Nicotine	Nornicotine	Anabasine	Anatabine	Alkaloids	% Anatabine
Variety	Seed ID	Plant ID	(%/g dry wt)	(%/g dry wt)	(%/g dry wt)	(%/g dry wt)	(%/g dry wt)	(%/g dry wt)
FC401	MS108	08GH97	1.46	0.0412	0.00429	0.0115	1.517	0.76
mutant 1	(dMS932)
FC401	MS445	08GH361	2.15	0.136	0.00423	0.0216	2.312	0.93
mutant 2
FC 401	MS170	08GH153	1.190	0.0224	0.00420	0.0084	2.312	0.93
mutant 3
FC 401	FC401	08GH1625	1.97	0.0476	0.0102	0.0875	2.115	4.41
control	Control
TN90	MS3908	09MN8938	4.08	0.092	0.0047	0.021	4.198	0.51
mutant 1
TN90	TN90 LC	09N26	4.44	0.118	0.0129	0.123	4.694	2.62
control	Control

FIG. 3 shows consistently low anatabine levels in mutagenized lines of the FC401 tobacco strain through multiple generations. Note that the data in M2 is from a single plant, while M3 and M4 are average values from multiple plants. FIG. 4 shows consistently low anatabine levels in a mutagenized line of the Tennessee Burley 90 (TN90) strain through multiple generations. As with FIG. 3, the data in M2 is from a single plant, while M3 is data of average values from multiple plants.

FIG. 5 shows the result of 750 M2 plants screened using High Performance Thin Layer Chromatography (HPTLC). 12 plants were selected during initial screening and mutants containing the least anatabine are presented. Control plants: Total alkaloid content in FC401 is 2-3%; percent anatabine is 2.5-3% and NAT ranges from 0.2-0.4 PPM. Anatabine mutant: Total alkaloid content 3.16%; percent anatabine 0.5% and NAT is 0.051%. i.e˜over 80 percent reduction.

While the foregoing has been described in detail with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications may be made, and equivalents thereof employed, without departing from the scope of the claims.

All of the above-mentioned references are herein incorporated by reference in their entirety to the same extent as if each individual reference was specifically and individually indicated to be incorporated herein by reference in its entirety.

DEPOSIT INFORMATION

A deposit of the proprietary inbred plant lines disclosed above and recited in the appended claims have been made with American Type Culture Collection (ATCC), 10801 University Boulevard, Manassas, Va. 20110, USA. The date of deposit for dMS932 was Mar. 19, 2018. The deposits of 2500 seeds for this variety was taken from the same deposits maintained since prior to the filing date of this application. Upon issuance of a patent, all restrictions upon the deposits will be irrevocably removed, and the deposits are intended by applicant to meet all of the requirements of 37 C.F.R. § 1.801 1.809. The ATCC has issued the accession number: ATCC Accession No. PTA-124990 for dMS932. This deposit will be maintained in the depository for a period of 30 years, or 5 years after the last request, or for the effective life of the patent, whichever is longer, and will be replaced as necessary during that period. Applicant does not waive any infringement of their rights granted under this patent or under the plant variety protection act (7 U.S.C. 2321 et seq.).

Claims

1. A tobacco plant, or a portion or a part thereof, of tobacco plant line dMS932, wherein a representative sample of seed of said tobacco plant is deposited under ATCC Accession Number PTA-124990.

2. The plant part of claim 1 selected from the group consisting of leaves, stems, veins, cuttings, and seeds.

3. A consumable tobacco product comprising the plant, or the portion or the part thereof, of claim 1.

4. The consumable tobacco product of claim 3, wherein said product is selected from the group consisting of a cigarette and a smokeless tobacco product.

5. A tobacco plant, or a portion or a part thereof, having all of the physiological and morphological characteristics of the tobacco plant of claim 1.

6. A method of producing tobacco seed, comprising crossing the plant of claim 1 with itself or a second tobacco plant and collecting resulting seed.

7. A F1 seed produced by the method of claim 6.

8. A tobacco plant produced by growing the resulting seed of claim 6.

9. A consumable tobacco product comprising the plant of claim 8, or a part or a portion thereof.

10. The consumable tobacco product of claim 9, wherein said product is selected from the group consisting of a cigarette and a smokeless tobacco product.

11. The tobacco plant of claim 8, wherein the produced tobacco plant comprises equal to or less than 0.0115 milligrams anatabine per gram of dry weight in leaf tissue.

12. The method of claim 6, further comprising backcrossing a progeny resulting from said crossing.

13. The method of claim 6, wherein the second tobacco plant comprises low nornicotine levels in dried leaves, wherein a tobacco plant produced by growing the resulting seed has 40% less tobacco-specific nitrosamines compared to Flue-cured variety ‘401’ tobacco plants.

14. A tobacco plant produced by growing the resulting seed of claim 13.

15. A consumable tobacco product comprising the plant of claim 14, or a part or a portion thereof.

16. The consumable tobacco product of claim 15, wherein said product is selected from the group consisting of a cigarette and a smokeless tobacco product.